Clinical Laboratory Analysis of Immunoglobulin Heavy Chain Variable Region Genes for Chronic Lymphocytic Leukemia Prognosis

Por Szankasi, Philippe, Bahler, David W.
Publicado em 2010

Immunomagnetic Bead Separation of Mononuclear Cells from Contaminating Granulocytes in Cryopreserved Blood Samples

Por Preobrazhensky, Sergey N., Bahler, David W.
Publicado em 2009

A New DNA-Based Test for Detection of Nucleophosmin Exon 12 Mutations by Capillary Electrophoresis

Por Szankasi, Philippe, Jama, Mohamed, Bahler, David W.
Publicado em 2008

Splenic Marginal Zone Lymphomas Appear to Originate from Different B Cell Types

Por Bahler, David W., Pindzola, J. Ander, Swerdlow, Steven H.
Publicado em 2002

Histological and Immunoglobulin VH Gene Analysis of Interfollicular Small Lymphocytic Lymphoma Provides Evidence for Two Types

Por Bahler, David W., Aguilera, Nadine S., Chen, Carolyn C., Abbondanzo, Susan L., Swerdlow, Steven H.
Publicado em 2000

Use of Similar Immunoglobulin VH Gene Segments by MALT Lymphomas of the Ocular Adnexa

Por Bahler, David W., Szankasi, Philippe, Kulkarni, Sucheta, Tubbs, Raymond R., Cook, James R., Swerdlow, Steven H.
Publicado em 2009

Expression of T-plastin, FoxP3 and other tumor-associated markers by leukemic T-cells of cutaneous T-cell lymphoma

Por CAPRIOTTI, ELISABETTA, VONDERHEID, ERIC C., THOBURN, CHRISTOPHER J., WASIK, MARIUSZ A., BAHLER, DAVID W., HESS, ALLAN D.
Publicado em 2008

Recurrent reciprocal RNA chimera involving YPEL5 and PPP1CB in chronic lymphocytic leukemia

Por Velusamy, Thirunavukkarasu, Palanisamy, Nallasivam, Kalyana-Sundaram, Shanker, Sahasrabuddhe, Anagh Anant, Maher, Christopher A., Robinson, Daniel R., Bahler, David W., Cornell, Timothy T., Wilson, Thomas E., Lim, Megan S., Chinnaiyan, Arul M., Elenitoba-Johnson, Kojo S. J.
Publicado em 2013

Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma

Por Kiel, Mark J., Velusamy, Thirunavukkarasu, Betz, Bryan L., Zhao, Lili, Weigelin, Helmut G., Chiang, Mark Y., Huebner-Chan, David R., Bailey, Nathanael G., Yang, David T., Bhagat, Govind, Miranda, Roberto N., Bahler, David W., Medeiros, L. Jeffrey, Lim, Megan S., Elenitoba-Johnson, Kojo S.J.
Publicado em 2012

Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK–STAT pathway in Sézary syndrome

Por Kiel, Mark J., Sahasrabuddhe, Anagh A., Rolland, Delphine C. M., Velusamy, Thirunavukkarasu, Chung, Fuzon, Schaller, Matthew, Bailey, Nathanael G., Betz, Bryan L., Miranda, Roberto N., Porcu, Pierluigi, Byrd, John C., Jeffrey Medeiros, L., Kunkel, Steven L., Bahler, David W., Lim, Megan S., Elenitoba-Johnson, Kojo S. J.
Publicado no Nat Commun (2015)

Whole-Genome Scanning by Array Comparative Genomic Hybridization as a Clinical Tool for Risk Assessment in Chronic Lymphocytic Leukemia

Por Gunn, Shelly R., Mohammed, Mansoor S., Gorre, Mercedes E., Cotter, Philip D., Kim, Jaeweon, Bahler, David W., Preobrazhensky, Sergey N., Higgins, Russell A., Bolla, Aswani R., Ismail, Sahar H., de Jong, Daphne, Eldering, Eric, van Oers, Marinus H.J., Mellink, Clemens H.M., Keating, Michael J., Schlette, Ellen J., Abruzzo, Lynne V., Robetorye, Ryan S.
Publicado em 2008